BRPI0414570A - 2-pyridone derivatives as neutrophil elastase inhibitors and their use - Google Patents
2-pyridone derivatives as neutrophil elastase inhibitors and their useInfo
- Publication number
- BRPI0414570A BRPI0414570A BRPI0414570-4A BRPI0414570A BRPI0414570A BR PI0414570 A BRPI0414570 A BR PI0414570A BR PI0414570 A BRPI0414570 A BR PI0414570A BR PI0414570 A BRPI0414570 A BR PI0414570A
- Authority
- BR
- Brazil
- Prior art keywords
- elastase inhibitors
- neutrophil elastase
- pyridone derivatives
- compounds
- pyridone
- Prior art date
Links
- 102000002255 Secretory Proteinase Inhibitory Proteins Human genes 0.000 title abstract 2
- 108010000303 Secretory Proteinase Inhibitory Proteins Proteins 0.000 title abstract 2
- 239000003591 leukocyte elastase inhibitor Substances 0.000 title abstract 2
- UBQKCCHYAOITMY-UHFFFAOYSA-N pyridin-2-ol Chemical class OC1=CC=CC=N1 UBQKCCHYAOITMY-UHFFFAOYSA-N 0.000 title abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 239000003602 elastase inhibitor Substances 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 230000003287 optical effect Effects 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 238000002560 therapeutic procedure Methods 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/81—Amides; Imides
- C07D213/82—Amides; Imides in position 3
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/84—Nitriles
- C07D213/85—Nitriles in position 3
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Peptides Or Proteins (AREA)
- Pyridine Compounds (AREA)
Abstract
"DERIVADOS DE 2-PIRIDONA COMO INIBIDORES DE ELASTASE DE NEUTRóFILO E SEU USO". A invenção provê novos compostos de fórmula (I) onde R¬ 1¬, R¬ 2¬, R¬ 4¬, R¬ 5¬, G¬ 1¬, G¬ 2¬, L, Y e n são como definidos no relatório descritivo, e isómeros óticos, racematos e tautómeros destes, e sais farmaceuticamente aceitáveis destes; juntamente com processos para sua preparação, composições os contendo e seu uso em terapia. Os compostos são inibidores da elastase de neutrófilo."2-PYRIDONE DERIVATIVES AS NEUTROPHYLE ELASTASE INHIBITORS AND THEIR USE". The invention provides novel compounds of formula (I) wherein R¬1¬, R¬2¬, R¬4¬, R¬5¬, G¬1¬, G¬2¬, L, Y and n are as defined in the report. descriptive, and optical isomers, racemates and tautomers thereof, and pharmaceutically acceptable salts thereof; together with processes for their preparation, compositions containing them and their use in therapy. The compounds are neutrophil elastase inhibitors.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE0302487A SE0302487D0 (en) | 2003-09-18 | 2003-09-18 | Novel compounds |
| PCT/SE2004/001336 WO2005026124A1 (en) | 2003-09-18 | 2004-09-15 | 2-pyridone derivatives as netrophil elastase inhibitors and their use |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BRPI0414570A true BRPI0414570A (en) | 2006-11-07 |
Family
ID=29212489
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BRPI0414570-4A BRPI0414570A (en) | 2003-09-18 | 2004-09-15 | 2-pyridone derivatives as neutrophil elastase inhibitors and their use |
Country Status (25)
| Country | Link |
|---|---|
| US (1) | US20070043036A1 (en) |
| EP (1) | EP1663974B1 (en) |
| JP (1) | JP2007505902A (en) |
| KR (1) | KR20060096995A (en) |
| CN (1) | CN100439339C (en) |
| AR (1) | AR046083A1 (en) |
| AT (1) | ATE420861T1 (en) |
| AU (1) | AU2004272485B2 (en) |
| BR (1) | BRPI0414570A (en) |
| CA (1) | CA2538410A1 (en) |
| CO (1) | CO5670357A2 (en) |
| DE (1) | DE602004019110D1 (en) |
| ES (1) | ES2319300T3 (en) |
| IL (1) | IL173986A0 (en) |
| IS (1) | IS8394A (en) |
| MX (1) | MXPA06002723A (en) |
| NO (1) | NO20061700L (en) |
| RU (1) | RU2348617C2 (en) |
| SA (1) | SA04250300B1 (en) |
| SE (1) | SE0302487D0 (en) |
| TW (1) | TW200526579A (en) |
| UA (1) | UA84878C2 (en) |
| UY (1) | UY28513A1 (en) |
| WO (1) | WO2005026124A1 (en) |
| ZA (1) | ZA200602262B (en) |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| TW200500341A (en) * | 2002-11-12 | 2005-01-01 | Astrazeneca Ab | Novel compounds |
| SE0302486D0 (en) | 2003-09-18 | 2003-09-18 | Astrazeneca Ab | Novel compounds |
| US7459562B2 (en) | 2004-04-23 | 2008-12-02 | Bristol-Myers Squibb Company | Monocyclic heterocycles as kinase inhibitors |
| TW200538453A (en) | 2004-04-26 | 2005-12-01 | Bristol Myers Squibb Co | Bicyclic heterocycles as kinase inhibitors |
| US7439246B2 (en) | 2004-06-28 | 2008-10-21 | Bristol-Myers Squibb Company | Fused heterocyclic kinase inhibitors |
| US7432373B2 (en) | 2004-06-28 | 2008-10-07 | Bristol-Meyers Squibb Company | Processes and intermediates useful for preparing fused heterocyclic kinase inhibitors |
| US20050288290A1 (en) | 2004-06-28 | 2005-12-29 | Borzilleri Robert M | Fused heterocyclic kinase inhibitors |
| TW200700392A (en) * | 2005-03-16 | 2007-01-01 | Astrazeneca Ab | Novel compounds |
| AP2007004244A0 (en) | 2005-05-10 | 2007-12-31 | Intermune Inc | Method of modulating stress-activated protein kinase system |
| RU2442771C2 (en) | 2005-08-08 | 2012-02-20 | Арджента Дискавери Лтд | Derivants of bicyclo[2, 2, 1] hept-7-ylamine and their applications |
| GB0516313D0 (en) | 2005-08-08 | 2005-09-14 | Argenta Discovery Ltd | Azole derivatives and their uses |
| CA2623957A1 (en) * | 2005-09-29 | 2007-04-05 | University Of Alberta | Compositions for and methods of granzyme b inhibition |
| GB0605469D0 (en) * | 2006-03-17 | 2006-04-26 | Argenta Discovery Ltd | Multimers of heterocyclic compounds and their use |
| TW200808763A (en) * | 2006-05-08 | 2008-02-16 | Astrazeneca Ab | Novel compounds I |
| TW200808771A (en) * | 2006-05-08 | 2008-02-16 | Astrazeneca Ab | Novel compounds II |
| JP5483880B2 (en) | 2006-10-23 | 2014-05-07 | 武田薬品工業株式会社 | Iminopyridine derivatives and uses thereof |
| KR101390076B1 (en) | 2006-11-08 | 2014-04-29 | 브리스톨-마이어스 스큅 컴퍼니 | Pyridinone compounds |
| WO2009061271A1 (en) * | 2007-11-06 | 2009-05-14 | Astrazeneca Ab | Some 2-pyrazinone derivatives and their use as inhibitors of neutrophile elastase |
| JP5327762B2 (en) | 2007-12-14 | 2013-10-30 | プルマジェン セラピューティクス(アズマ)リミテッド | Indole and its therapeutic use |
| EA017736B1 (en) | 2008-01-23 | 2013-02-28 | Бристол-Маерс Сквибб Компани | 4-pyridinone compounds and their use for cancer |
| US8481569B2 (en) | 2008-04-23 | 2013-07-09 | Takeda Pharmaceutical Company Limited | Iminopyridine derivatives and use thereof |
| EP2296653B1 (en) | 2008-06-03 | 2016-01-27 | Intermune, Inc. | Compounds and methods for treating inflammatory and fibrotic disorders |
| BRPI1005327A2 (en) | 2009-02-17 | 2019-09-24 | Chiesi Farm Spa | triazolopyridine derivatives as p38 map kinase inhibitors |
| GB0902648D0 (en) | 2009-02-17 | 2009-04-01 | Argenta Discovery Ltd | Pharmaceutical compounds and compositions |
| TW201036957A (en) | 2009-02-20 | 2010-10-16 | Astrazeneca Ab | Novel salt 628 |
| AU2010302420B2 (en) * | 2009-10-02 | 2013-07-04 | Astrazeneca Ab | 2-pyridone compounds used as inhibitors of neutrophil elastase |
| GB0918924D0 (en) | 2009-10-28 | 2009-12-16 | Vantia Ltd | Azaindole derivatives |
| GB0918923D0 (en) | 2009-10-28 | 2009-12-16 | Vantia Ltd | Aminothiazole derivatives |
| GB0918922D0 (en) | 2009-10-28 | 2009-12-16 | Vantia Ltd | Aminopyridine derivatives |
| IN2012DN05081A (en) * | 2009-12-08 | 2015-10-09 | Boehringer Ingelheim Int | |
| GB201009731D0 (en) | 2010-06-10 | 2010-07-21 | Pulmagen Therapeutics Inflamma | Kinase inhibitors |
| JP5709999B2 (en) | 2011-08-01 | 2015-04-30 | 大日本住友製薬株式会社 | Uracil derivatives and their pharmaceutical use |
| SG11201402985VA (en) | 2011-12-09 | 2014-08-28 | Chiesi Farma Spa | Kinase inhibitors |
| BR112014013178A2 (en) | 2011-12-09 | 2017-06-13 | Chiesi Farm Spa | compound, pharmaceutical composition and use of a compound |
| MY167216A (en) | 2011-12-09 | 2018-08-14 | Chiesi Farm Spa | Kinase inhibitors |
| US20140057920A1 (en) | 2012-08-23 | 2014-02-27 | Boehringer Ingelheim International Gmbh | Substituted 4-pyridones and their use as inhibitors of neutrophil elastase activity |
| US20140057926A1 (en) | 2012-08-23 | 2014-02-27 | Boehringer Ingelheim International Gmbh | Substituted 4-pyridones and their use as inhibitors of neutrophil elastase activity |
| US9102624B2 (en) | 2012-08-23 | 2015-08-11 | Boehringer Ingelheim International Gmbh | Substituted 4-pyridones and their use as inhibitors of neutrophil elastase activity |
| AR092742A1 (en) | 2012-10-02 | 2015-04-29 | Intermune Inc | ANTIFIBROTIC PYRIDINONES |
| RU2015151886A (en) | 2013-06-06 | 2017-06-08 | КЬЕЗИ ФАРМАЧЕУТИЧИ С.п.А. | KINAZ INHIBITORS |
| US9221807B2 (en) * | 2014-02-21 | 2015-12-29 | Boehringer Ingelheim International Gmbh | Substituted pyridones and pyrazinones and their use as inhibitors of neutrophil elastase activity |
| RU2692485C2 (en) | 2014-04-02 | 2019-06-25 | Интермьюн, Инк. | Antifibrous pyridinones |
| MA43940A (en) | 2015-09-02 | 2018-12-12 | Glaxosmithkline Ip No 2 Ltd | PYRIDINONE DICARBOXAMIDE USED AS A BROMODOMAIN INHIBITOR |
| TW201720828A (en) | 2015-11-23 | 2017-06-16 | 赫孚孟拉羅股份公司 | Therapeutic compounds and compositions, and methods of use thereof |
| AR107163A1 (en) | 2015-12-23 | 2018-03-28 | Chiesi Farm Spa | QUINASE INHIBITORS |
| TW201730189A (en) | 2015-12-23 | 2017-09-01 | 吉斯藥品公司 | Kinase inhibitors |
| MA44131A (en) | 2015-12-23 | 2021-05-26 | Chiesi Farm Spa | DERIVATIVES OF 1- (3-TERT-BUTYL-2H-PYRAZOL-5-YL OR 5-TERT-BUTYL-ISOXAOL-3-YL) -3- (4 - ([1,2,4] TRIAZOLO [4,3 -A] PYRIDIN-6-YLOXY) -1,2,3,4-TETRAHYDRO-NAPHTHALENYL) UREA AND THEIR USE AS P38 MAPK INHIBITORS |
| JP7034942B2 (en) | 2016-05-05 | 2022-03-14 | エフ.ホフマン-ラ ロシュ アーゲー | Pyrazole derivatives, their compositions and therapeutic uses |
| BR112019004486A2 (en) | 2016-09-06 | 2019-05-28 | F.Hoffmann-La Roche Ag | 8- (azetidin-1-yl) - [1,2,4] triazolo [1,5a] pyridinyl compounds, compositions and methods of use |
| MX2019007339A (en) | 2016-12-29 | 2019-09-06 | Hoffmann La Roche | PYRAZOLOPYRIMIDINE COMPOUNDS AND METHODS OF USING THEM. |
| JP2020510061A (en) | 2017-03-14 | 2020-04-02 | エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft | Pyrazolochlorophenyl compounds, compositions and methods of using same |
| JP7256757B2 (en) | 2017-05-22 | 2023-04-12 | エフ. ホフマン-ラ ロシュ アーゲー | Therapeutic compounds and compositions, and methods of their use |
| WO2018215390A1 (en) | 2017-05-22 | 2018-11-29 | F. Hoffmann-La Roche Ag | Therapeutic compounds and compositions, and methods of use thereof |
| US10364245B2 (en) | 2017-06-07 | 2019-07-30 | Chiesi Farmaceutici S.P.A. | Kinase inhibitors |
| WO2019139714A1 (en) | 2018-01-15 | 2019-07-18 | Genentech, Inc. | Pyrazolopyrimidine compounds as jak inhibitors |
| CN111683976B (en) | 2018-02-05 | 2022-11-18 | 生物辐射实验室股份有限公司 | Chromatography resins with anion-exchange-hydrophobic mixed-mode ligands |
| KR102915019B1 (en) | 2019-04-24 | 2026-01-21 | 바이엘 악티엔게젤샤프트 | 4H-pyrrolo[3,2-c]pyridin-4-one compound |
| CN110192947B (en) * | 2019-05-28 | 2022-01-04 | 河南省超亚医药器械有限公司 | Infant lung hot compress patch |
| CN110192948B (en) * | 2019-05-28 | 2022-01-04 | 河南省超亚医药器械有限公司 | Infant abdomen hot compress patch |
| CN114026096B (en) | 2019-06-18 | 2025-02-07 | 豪夫迈·罗氏有限公司 | Tetrazolyl-substituted pyrazolopyrimidine JAK kinase inhibitors and uses thereof |
| EP3986899A1 (en) | 2019-06-18 | 2022-04-27 | F. Hoffmann-La Roche AG | Pyrazolopyrimidine aryl ether inhibitors of jak kinases and uses thereof |
| JP7657740B2 (en) | 2019-06-18 | 2025-04-07 | エフ・ホフマン-ラ・ロシュ・アクチェンゲゼルシャフト | PYRAZOLOPYRIMIDINE SULFONE INHIBITORS OF JAK KINASES AND USES THEREOF - Patent application |
| AU2020349353A1 (en) | 2019-09-17 | 2022-04-14 | Duke University | Alvelestat for use in the treatment of graft rejection, bronchiolitis obliterans syndrome and graft versus host disease |
| HUE064089T2 (en) | 2020-04-16 | 2024-02-28 | Mereo Biopharma 4 Ltd | Methods involving neutrophil elastase inhibitor alvelestat for treating respiratory disease mediated by alpha-1 antitrypsin deficiency |
| AU2022373971A1 (en) | 2021-10-20 | 2024-04-04 | Mereo Biopharma 4 Limited | Neutrophil elastase inhibitors for use in the treatment of fibrosis |
| CN114057630B (en) * | 2021-12-23 | 2023-06-02 | 郑州大学 | Pirfenidone derivatives and their synthetic methods and applications |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5521179A (en) * | 1991-04-18 | 1996-05-28 | Zeneca Limited | Heterocyclic amides |
| GB9207145D0 (en) * | 1991-04-18 | 1992-05-13 | Ici Plc | Heterocyclic amides |
| FR2687674B1 (en) * | 1992-02-07 | 1995-05-19 | Roussel Uclaf | NEW PYRIDONE DERIVATIVES, THEIR PREPARATION PROCESS, THE NEW INTERMEDIATES OBTAINED, THEIR APPLICATION AS MEDICAMENTS AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING THEM. |
| EP0729464A1 (en) * | 1993-11-19 | 1996-09-04 | PARKE, DAVIS & COMPANY | 5,6-dihydropyrone derivatives as protease inhibitors and antiviral agents |
| RU2067579C1 (en) * | 1994-10-07 | 1996-10-10 | Пермский фармацевтический институт | 3-(2'-naphthoylmethylene)-piperazinone-2 and 1-n-phenyl-3-phenacylidenepiperazinone-2 showing antiinflammatory activity |
| DE60139506D1 (en) * | 2000-12-28 | 2009-09-17 | Shionogi & Co | 2-PYRIDONE DERIVATIVES WITH AFFINITY FOR THE CANNABINOID TYPE-2 RECEPTOR |
| GB0129260D0 (en) * | 2001-12-06 | 2002-01-23 | Eisai London Res Lab Ltd | Pharmaceutical compositions and their uses |
| AU2002361992A1 (en) * | 2001-12-20 | 2003-07-09 | Bayer Aktiengesellschaft | 1,4-dihydro-1,4-diphenylpyridine derivatives |
| GB2383326A (en) * | 2001-12-20 | 2003-06-25 | Bayer Ag | Antiinflammatory dihydropyridines |
| TW200500341A (en) * | 2002-11-12 | 2005-01-01 | Astrazeneca Ab | Novel compounds |
| SE0302486D0 (en) * | 2003-09-18 | 2003-09-18 | Astrazeneca Ab | Novel compounds |
-
2003
- 2003-09-18 SE SE0302487A patent/SE0302487D0/en unknown
-
2004
- 2004-09-13 TW TW093127678A patent/TW200526579A/en unknown
- 2004-09-15 AU AU2004272485A patent/AU2004272485B2/en not_active Ceased
- 2004-09-15 AT AT04775439T patent/ATE420861T1/en not_active IP Right Cessation
- 2004-09-15 CN CNB2004800275174A patent/CN100439339C/en not_active Expired - Fee Related
- 2004-09-15 WO PCT/SE2004/001336 patent/WO2005026124A1/en not_active Ceased
- 2004-09-15 UA UAA200602252A patent/UA84878C2/en unknown
- 2004-09-15 ES ES04775439T patent/ES2319300T3/en not_active Expired - Lifetime
- 2004-09-15 MX MXPA06002723A patent/MXPA06002723A/en unknown
- 2004-09-15 US US10/572,640 patent/US20070043036A1/en not_active Abandoned
- 2004-09-15 JP JP2006526856A patent/JP2007505902A/en active Pending
- 2004-09-15 BR BRPI0414570-4A patent/BRPI0414570A/en not_active IP Right Cessation
- 2004-09-15 DE DE602004019110T patent/DE602004019110D1/en not_active Expired - Fee Related
- 2004-09-15 KR KR1020067005458A patent/KR20060096995A/en not_active Withdrawn
- 2004-09-15 RU RU2006112427/04A patent/RU2348617C2/en not_active IP Right Cessation
- 2004-09-15 EP EP04775439A patent/EP1663974B1/en not_active Expired - Lifetime
- 2004-09-15 UY UY28513A patent/UY28513A1/en unknown
- 2004-09-15 CA CA002538410A patent/CA2538410A1/en not_active Abandoned
- 2004-09-17 AR ARP040103354A patent/AR046083A1/en not_active Application Discontinuation
- 2004-09-18 SA SA4250300A patent/SA04250300B1/en unknown
-
2006
- 2006-02-27 IL IL173986A patent/IL173986A0/en unknown
- 2006-03-15 CO CO06026211A patent/CO5670357A2/en not_active Application Discontinuation
- 2006-03-17 ZA ZA200602262A patent/ZA200602262B/en unknown
- 2006-03-31 IS IS8394A patent/IS8394A/en unknown
- 2006-04-18 NO NO20061700A patent/NO20061700L/en not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| ATE420861T1 (en) | 2009-01-15 |
| IL173986A0 (en) | 2006-07-05 |
| CO5670357A2 (en) | 2006-08-31 |
| KR20060096995A (en) | 2006-09-13 |
| CN1856467A (en) | 2006-11-01 |
| AU2004272485B2 (en) | 2008-03-13 |
| RU2348617C2 (en) | 2009-03-10 |
| AR046083A1 (en) | 2005-11-23 |
| DE602004019110D1 (en) | 2009-03-05 |
| IS8394A (en) | 2006-03-31 |
| UY28513A1 (en) | 2005-04-29 |
| JP2007505902A (en) | 2007-03-15 |
| ZA200602262B (en) | 2007-07-25 |
| CA2538410A1 (en) | 2005-03-24 |
| WO2005026124A1 (en) | 2005-03-24 |
| SA04250300B1 (en) | 2008-09-07 |
| SE0302487D0 (en) | 2003-09-18 |
| CN100439339C (en) | 2008-12-03 |
| AU2004272485A1 (en) | 2005-03-24 |
| NO20061700L (en) | 2006-04-18 |
| UA84878C2 (en) | 2008-12-10 |
| HK1089167A1 (en) | 2006-11-24 |
| MXPA06002723A (en) | 2006-06-06 |
| RU2006112427A (en) | 2007-11-10 |
| ES2319300T3 (en) | 2009-05-06 |
| US20070043036A1 (en) | 2007-02-22 |
| TW200526579A (en) | 2005-08-16 |
| EP1663974B1 (en) | 2009-01-14 |
| EP1663974A1 (en) | 2006-06-07 |
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